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List of works by Eric D. Green

2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries

scientific article

A Physical Map of Human Chromosome 7: An Integrated YAC Contig Map with Average STS Spacing of 79 kb ⬇️

scientific article published on July 1, 1997

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

scientific article

A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines

scientific article

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint

scientific article published in December 2001

A clinical decision support system for integrating tuberculosis and HIV care in Kenya: a human-centered design approach

scientific article

A collection of 1814 human chromosome 7-specific STSs

scientific article published in January 1997

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

scientific article

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

scientific article

A family of mammalian anion transporters and their involvement in human genetic diseases

scientific article

A high-resolution map of human evolutionary constraint using 29 mammals

scientific article

A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening

scientific article published on January 1995

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

scientific article

A mutation in PDS causes non-syndromic recessive deafness ⬇️

scientific article (publication date: March 1998)

A physical map of the human genome

scientific article

A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications

scientific article

A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo

scientific article

A rational approach to minimal high-resolution cross-reactive arrays

scientific article published in November 2006

A scalable and flexible approach for investigating the genomic landscapes of phylogenetic incongruence

scientific article

A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome

article

A vision for the future of genomics research ⬇️

scientific article published on April 14, 2003

Adaptive evolution of foundation kinetochore proteins in primates

scientific article

Aligning multiple genomic sequences with the threaded blockset aligner

scientific article (publication date: April 2004)

An effective approach for analyzing "prefinished" genomic sequence data

scientific article

An effective method for detecting gene conversion events in whole genomes

scientific article

An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval

scientific article

An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencing

scientific article (publication date: 29 March 2005)

An intermediate grade of finished genomic sequence suitable for comparative analyses

scientific article published on 12 October 2004

Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome

scientific article published in June 2007

Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome

scientific article

Analysis of the human herpesvirus 8 (HHV-8) genome and HHV-8 vIL-6 expression in archival cases of castleman disease at low risk for HIV infection

scientific article published on February 2002

Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.

scientific article published in October 2005

Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation

scientific article

Basic science: Bedrock of progress

scientific article published on March 2016

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

scientific article

Biomedical research. The genome project: what will it do as a teenager? Interview by Jocelyn Kaiser

scientific article published in February 2011

Birth-and-death of KLK3 and KLK2 in primates: evolution driven by reproductive biology

scientific article published on January 2012

CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR.

scientific article

Calcium channels light up.

scientific article published in July 2007

Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies

scientific article published in October 2001

Characterizing genetic variants for clinical action

scientific article

Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels

scientific article

Charting a course for genomic medicine from base pairs to bedside

scientific article published on February 2011

Chemotherapy and radiotherapy for treatment of cutaneous lymphoma in a ground cuscus (Phalanger gymnotis).

scientific article published in September 2008

Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.

scientific article published in December 2000

Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus

scientific article (publication date: June 2011)

Comparative genome mapping in the sequence-based era: early experience with human chromosome 7.

scientific article

Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes

scientific article

Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.

scientific article

Comparative sequence analyses reveal rapid and divergent evolutionary changes of the WFDC locus in the primate lineage

scientific article (publication date: March 2007)

Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome

scientific article

Comparative sequence analysis of a single-gene conserved segment in mouse and human

scientific article

Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event

scientific article published on 24 October 2008

Comparative sequence analysis of the Gdf6 locus reveals a duplicon-mediated chromosomal rearrangement in rodents and rapidly diverging coding and regulatory sequences

scientific article

Comparative sequencing provides insights about the structure and conservation of marsupial and monotreme genomes

scientific article

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

scientific article

Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy

scientific article

Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene

scientific article (publication date: 2001)

Computational reconstruction of ancestral DNA sequences

scientific article published in January 2008

Confirming the phylogeny of mammals by use of large comparative sequence data sets

scientific article

Conversion events in gene clusters

scientific article

Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.

scientific article

Data use under the NIH GWAS data sharing policy and future directions

scientific article published in September 2014

Defining functional DNA elements in the human genome

scientific article

Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site

scientific article

Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome

scientific article published on 5 December 2005

Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension

scientific article published on 18 August 2003

Detection and characterization of chimeric yeast artificial-chromosome clones ⬇️

scientific article published on November 1, 1991

Detection of potential GDF6 regulatory elements by multispecies sequence comparisons and identification of a skeletal joint enhancer

scientific article published in September 2005

Dietary Cl(-) restriction upregulates pendrin expression within the apical plasma membrane of type B intercalated cells

scientific article published on 2 May 2006

Differences between pair-wise and multi-sequence alignment methods affect vertebrate genome comparisons

scientific article

Direct interaction of Sox10 with the promoter of murine Dopachrome Tautomerase (Dct) and synergistic activation of Dct expression with Mitf

scientific article

Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype

scientific journal article

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

scientific article

Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty

scientific article

Distribution and intensity of constraint in mammalian genomic sequence

scientific article (publication date: July 2005)

Dynamic evolution of V1R putative pheromone receptors between Mus musculus and Mus spretus

scientific article

Effects of extensive circumferential periosteal stripping on the microstructure and mechanical properties of the murine femoral cortex

scientific article published on 16 September 2011

Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte

scientific article

Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates

scientific article (publication date: 11 January 2010)

Erratum: Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

scholarly article published in Nature Genetics

Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

scholarly article published in Molecular Psychiatry

Erratum: Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22

article

Esophageal diverticulum associated with a trichobezoar in a cat.

scientific article

Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer

scientific article published on 3 November 2005

Evolution of siglec-11 and siglec-16 genes in hominins

scientific article

Evolutionary history reconstruction for Mammalian complex gene clusters

scientific article

Examining How Race, Ethnicity, and Ancestry Data Are Used in Biomedical Research

scientific article published in The Journal of the American Medical Association

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

scientific article published in July 1992

Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein

scientific article published in November 2002

Functional expression of yeast artificial chromosome-human multidrug resistance genes in mouse cells

scientific article

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

scientific article published on 10 October 2006

Gene expression profiles in acute myeloid leukemia with common translocations using SAGE.

scientific article published on 17 January 2006

Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model

scientific article

Gene-environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop

scientific article

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

scientific article

Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome

scientific article

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

scientific article

Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4.

scientific article published in September 2002

Genome sequence of the Brown Norway rat yields insights into mammalian evolution

scientific article

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

scientific article

Genomic Medicine Year in Review: 2019

scientific article published on 05 December 2019

Genomic Medicine Year in Review: 2020

scientific article published on 01 December 2020

Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor ⬇️

scientific article published on January 1, 2002

Genomic variation in multigenic traits: Hirschsprung disease

scientific article published in January 2003

Genomics Education for Health Care Professionals in the 21st Century ⬇️

scientific article published on September 7, 2011

Genomics Reaches the Clinic: From Basic Discoveries to Clinical Impact ⬇️

scientific article published on September 30, 2011

Global implementation of genomic medicine: We are not alone

scientific article

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

scientific article

Gpnmb is a melanoblast-expressed, MITF-dependent gene

scientific article

High Throughput Fingerprint Analysis of Large-Insert Clones ⬇️

scientific article published on November 1, 1997

Human Genome Project: Twenty-five years of big biology

scientific article

Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome

scientific article published in October 2004

Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint

scientific article published on July 1999

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

scientific article published in June 2007

Identification and characterization of multi-species conserved sequences

scientific article

Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS)

scientific article (publication date: February 1999)

Identification of 3'-terminal exons from yeast artificial chromosomes ⬇️

scientific article published on June 1, 1995

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

scientific article

Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4.

scientific article

Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines

scientific article

Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish

scientific article

Identification of pendrin as a common mediator for mucus production in bronchial asthma and chronic obstructive pulmonary disease

scientific article

Identification of the Otopetrin Domain, a conserved domain in vertebrate otopetrins and invertebrate otopetrin-like family members

scientific article

Identifying gene regulatory elements by genome-wide recovery of DNase hypersensitive sites

scientific article

Implementing Genomic Medicine in the Clinic

Implementing genomic medicine in the clinic: the future is here

scientific article published on 10 January 2013

In silico and functional studies of the regulation of the glucocerebrosidase gene

scientific article

Influencing the field. Interview by Kristie Nybo

scientific article published in February 2011

Initial sequencing and comparative analysis of the mouse genome

scientific article

Integrative DNA, RNA, and protein evidence connects TREML4 to coronary artery calcification

scientific article

Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice

scientific journal article

Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.

scientific article

Isolation of DNA from the centromere of human chromosome 7 by microdissection

scientific article published on June 1, 1997

Isolation, genomic structure and developmental expression of Fgf8 in the short-tailed fruit bat, Carollia perspicillata

scientific article

LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA

scientific article (publication date: April 2003)

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

scientific article

Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

scientific article published on 2 January 2007

Large-scale sequencing of the CD33-related Siglec gene cluster in five mammalian species reveals rapid evolution by multiple mechanisms

scientific article

Leading the way to genomic medicine

scientific article published on 11 March 2014

Lessons of the Northern Ireland Peace Process∗

Leukocyte adhesion deficiency (LAD) type II/carbohydrate deficient glycoprotein (CDG) IIc founder effect and genotype/phenotype correlation

scientific article

Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses

scientific article

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia

article

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

scientific article

Localization of 67 Exons on a YAC Contig Spanning 1.5 Mb around the Multidrug Resistance Gene Region of Human Chromosome 7q21.1 ⬇️

scientific article published on April 1, 1998

Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities

scientific article published in November 1996

Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes

scientific article

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

scientific article

MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia

scientific article

Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model

scientific article

Maintenance of hypomethylation status and preferential expression of exogenous humanMDR1/PGY1 gene in mouse L cells by YAC mediated transfer ⬇️

scientific article published on July 1, 1997

Maurice Green - A pioneering virologist

scientific article published on 9 January 2018

Mechanism of iodide/chloride exchange by pendrin

scientific article published on 20 May 2004

Meiotic arrest and aneuploidy in MLH3-deficient mice

scientific journal article

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

scientific article published on May 2008

Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

scientific article

Multi-species sequence comparison reveals dynamic evolution of the elastin gene that has involved purifying selection and lineage-specific insertions/deletions

scientific article

MultiPipMaker and supporting tools: Alignments and analysis of multiple genomic DNA sequences

scientific article

Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness

scientific article

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

scientific article (publication date: November 1999)

NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl- conservation

scientific article published on 11 October 2004

No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder

scientific article published in December 2001

Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function

scientific article published on 10 March 2005

Observations on the micromorphology of the tropical rat mite Ornithonyssus bacoti (Hirst) as revealed by scanning electron microscopy.

scientific article published on September 1996

Opening plenary speaker: Human genomics, precision medicine, and advancing human health

scientific article

Opportunities, resources, and techniques for implementing genomics in clinical care

scientific article published on 05 August 2019

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

scientific article

Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells

scientific journal article

Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells

scientific article

Pericentromeric duplications in the laboratory mouse

scientific article

Perspective: Sustaining the big-data ecosystem

scientific article

Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence

scientific article

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations

scientific article

Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15.

scientific article

Prepublication data sharing

scientific article

Prioritizing diversity in human genomics research.

scientific article published on 20 November 2017

Progressive proximal expansion of the primate X chromosome centromere

scientific article

Quantitative Estimates of Sequence Divergence for Comparative Analyses of Mammalian Genomes ⬇️

scientific article published on May 1, 2003

Recent Selection Changes in Human Genes under Long-Term Balancing Selection

scientific article published on February 2016

Reconstructing large regions of an ancestral mammalian genome in silico

scientific article

Reconstructing the Evolutionary History of Complex Human Gene Clusters

article

Recurrent duplication-driven transposition of DNA during hominoid evolution

scholarly article

Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice

scientific article published on 8 August 2007

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig

scientific article published on November 1995

Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea

scientific article published on November 1, 1997

Regulatory divergence modifies limb length between mammals

scientific article

Relevance of genomics to healthcare and nursing practice

scientific article published on 31 January 2013

Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease

scientific article published on August 2014

Reproduction and immunity-driven natural selection in the human WFDC locus

scientific article published on 4 January 2013

Research directions in the clinical implementation of pharmacogenomics - An Overview of US programs and projects

scientific article published on 20 February 2018

Research ethics. The complexities of genomic identifiability

scientific article published in January 2013

Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome

scientific article published in October 2002

Revealing mammalian evolutionary relationships by comparative analysis of gene clusters

scientific article

Sequence diversity of Pan troglodytes subspecies and the impact of WFDC6 selective constraints in reproductive immunity

scientific article published on January 2013

Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences ⬇️

scientific article published on November 1, 1991

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling

scientific article published on 3 May 2006

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder

scientific article published on 19 September 2007

Skin microbiome in health and disease.

scientific article

Special Issue Editors' Introduction: "Genomics and the Human Genome Project"

scientific article published on 01 December 2018

Specific inactivation of two immunomodulatory SIGLEC genes during human evolution

scientific article

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

scientific article published on September 2005

Straight talk with... Eric Green. Interview by Erica Westly

scientific article published in January 2010

Strategies for the systematic sequencing of complex genomes

scientific article

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

scientific article

Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artificial chromosomes ⬇️

scientific article published on November 1, 1991

Systematic sequencing of cDNA clones using the transposon Tn5

scientific article

TOWARDS COORDINATED INTERNATIONAL SUPPORT OF CORE DATA RESOURCES FOR THE LIFE SCIENCES

scientific article (publication date: 23 February 2017)

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

scientific article

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

scientific article published in January 2001

Targets of balancing selection in the human genome

scientific article published on 27 August 2009

The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map.

scientific article

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

scientific article published on 14 July 2009

The DNA sequence of human chromosome 7

scientific article

The NIH Big Data to Knowledge (BD2K) initiative

scientific article published on November 2015

The National Institutes of Health's Big Data to Knowledge (BD2K) initiative: capitalizing on biomedical big data

scientific article

The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4.

scientific article

The completion of the Mammalian Gene Collection (MGC).

scientific article published on 18 September 2009

The future of DNA sequencing

scientific article published in Nature

The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletion

scientific article

The human genome sequence expedition: views from the "base camp".

scientific article

The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7.

scientific article

The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variants

scientific article (publication date: October 2001)

The human reelin gene: isolation, sequencing, and mapping on chromosome 7.

scientific article

The impact of the 2014 Ebola virus disease outbreak in Liberia on parent preferences for harsh discipline practices: a quasi-experimental, pre-post design

scientific article published on 9 January 2018

The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour

scientific article

The role of aminoacyl-tRNA synthetases in genetic diseases

scientific article published on January 2008

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)

scientific article

The surface morphology of the omasum of the African goat.

scientific article published in September 1996

The value of avian genomics to the conservation of wildlife

scientific article (publication date: 14 July 2009)

Topographical and temporal diversity of the human skin microbiome

scientific article

Transcription-associated mutational asymmetry in mammalian evolution

scientific article

VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer ⬇️

scientific article published on December 30, 2011

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